Canonical Allele Identifier: PA2827241050
Gene: CYP7B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 363581
ClinVar RCV Id: RCV000319168 RCV001861331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311041.1:p.His340Tyr
CA4764088
NM_001324112.2:c.1018C>T